917207-79-5 Usage
Molecular weight
184.24 g/mol The molecular weight of the compound is 184.24 grams per mole.
Appearance
Yellow to brown solid The compound appears as a yellow to brown solid substance.
Usage
Synthesis of pharmaceuticals and agrochemicals 1-ETHYL-2-METHYL-1H-INDOLE-3-CARBONITRILE is used in the synthesis of various pharmaceutical and agrochemical products.
Bioactivity
Potential bioactivity The compound is known for its potential bioactivity, which may have applications in the development of new drugs or treatments.
Structure
Ethyl and methyl groups on the indole ring The compound's structure features an ethyl group and a methyl group attached to the indole ring.
Carbonitrile group
3-position on the ring The carbonitrile group is located at the 3-position of the indole ring, which may influence its chemical properties and reactivity.
Primary use
Intermediate in drug and agricultural chemical production 1-ETHYL-2-METHYL-1H-INDOLE-3-CARBONITRILE is mainly used as an intermediate in the production of various drugs and agricultural chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 917207-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,2,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 917207-79:
(8*9)+(7*1)+(6*7)+(5*2)+(4*0)+(3*7)+(2*7)+(1*9)=175
175 % 10 = 5
So 917207-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2/c1-3-14-9(2)11(8-13)10-6-4-5-7-12(10)14/h4-7H,3H2,1-2H3
917207-79-5Relevant articles and documents
GaCl3-Catalyzed C-H Cyanation of Indoles with N-Cyanosuccinimide
Wang, Xue,Makha, Mohamed,Chen, Shu-Wei,Zheng, Huaiji,Li, Yuehui
, p. 6199 - 6206 (2019/05/24)
An efficient GaCl3-catalyzed direct cyanation of indoles and pyrroles using bench-stable electrophilic cyanating agent N-cyanosuccinimide was achieved and afforded 3-cyanoindoles and 2-cyanopyrroles in good yields and excellent regioselectivities. Notably, this protocol exhibited high reactivity for unprotected indoles and was applicable to a broad range of indole and pyrrole substrates.
Cyanation of indoles with benzyl cyanide as the cyanide anion surrogate
Zhang, Lianpeng,Wen, Qiaodong,Jin, Jisong,Wang, Chen,Lu, Ping,Wang, Yanguang
, p. 4236 - 4240 (2013/06/26)
A copper-mediated direct cyanation of indoles with benzyl cyanide as the cyanide anion surrogate has been achieved. The cascade reaction furnished 3-cyanoindoles under mild reaction conditions in good to excellent yields with various functional groups tolerance.
